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Molecular mechanisms of the blood-brain barrier induction in cerebral blood vessels

Research Project

Project/Area Number 11670226
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Experimental pathology
Research InstitutionKeio University

Principal Investigator

IKEDA Eiji  Keio University, School of Medicine, Assistant Professor, 医学部, 専任講師 (30232177)

Co-Investigator(Kenkyū-buntansha) OKADA Yasunori  Keio University, School of Medicine, Professor, 医学部, 教授 (00115221)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1999: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsCerebral blood vessels / Blood-brain barrier / Blood-retinal barrier / VEGF / 個体発生
Research Abstract

Microenvironment of central nerve system is maintained by the b90 lood-brain barrier (BBB). The BBB is formed by the neural tissue-specific vascular endothelial cells. Using an in vivo model of BBB induction which is based on the xenograft transplantation between quail and chick embryos, we showed that, among the quail VEGF isoforms (in quail, VEGF_<122, 146, 166, 190>), VEGF_<146> expression is up-regulated exclusively in the embryonic brain tissues after the BBB differentiation initiated. This finding suggests the involvement of VEGF not only in the process of embryonic brain angiogenesis but also in that of BBB induction through the changes in its isoform expression pattern. Blood vessels in retina have a counterpart of BBB called the blood-retinal barrier (BRB), and the breakdown of BRB is noted in diabetic retinopathy. Then, in order to discuss the relationship between VEGF-VEGF receptors system and BRB function, we analysed the expression of VEGF isoforms (in human, VEGF_<121, 145, 165, 189, 206>) and its receptors (VEGF-R1, VEGF-R2, neuropilin-1) in intraocular lesions of the patients with diabetic retinopathy. When the expression patterns of VEGF isoforms and VEGF receptors are compared with the activity of the lesions, close correlation was observed between the high activity of lesions and the expression of VEGF_<165>, VEGF-R2 and neuropilin-1. Considering that neuropilin-1 is a VEGF_<165>-specific receptor to enhance the intracytoplasmic signalling from VEGF_<165> via VEGF-R2, our data suggested that VEGF_<165> plays an important role in the formation of retinal lesions in diabetic retinopathy. The above results obtained from the avian system as well as the human diabetic retinopathy lead us to the idea that VEGF is involved in the process of BBB induction through the changes in the isoform expression pattern.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Ishida S,Shinoda K,Kawashima S,Oguchi Y,Okada Y,Ikeda E: "Coexpression of VEGF receptors VEGF-R2 and neuropilin-1 in proliferative diabetic retinopathy."Invest Opthalmol Vis Sci. 41(7). 1649-1656 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Ishida S, Shinoda K, Kawashima S, Oguchi Y, Okada Y, Ikeda E: "Coexpression of VEGF receptors VEGF-R2 and neuropilin-1 in proliferative diabetic retinopathy"Invest Ophthalmol Vis Sci. 41 (7). 1649-1656 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Ishida S et al: "Coexpression of VEGF receptors VEGF-R2 and neuropilin-1 in proliferative diabetic retinopathy."Invest Ophthalmol Vis Sci. 41(7). 1649-56 (2000)

    • Related Report
      2000 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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